Aim: To provide an introduction to the GMP requirements for the formulation, scale up and optimization of Finished Solid Dose Forms and to develop a practical understanding of Process Mapping, Risk Analysis and Critical Control points, Validation requirements and Quality Plans as it applies to solid dose formulations.
Day 1 AM ►Granulation Technology and Control
PM ► Blending and Milling Technology and Control Changed CONTENT
Day 2 AM ►Encapsulation Technology and Control
PM ►Compression Technology and Control Recommended for:
Day 3 AM ►Coating Technology and Control
Production and Engineering
PM ►Packaging Technology and Control
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